Inventor
VINCENT JOHN B
CA28 patents
⚠️ This page may combine multiple inventors who share the name “VINCENT JOHN B”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.
UNIV ALABAMA
7 patentsUS6444231B2Sep 3, 2002
USE OF TRIAQUA-μ3-OXOHEXAKIS-μ-PROPIONATOTRICHROMIUM(1+), [CR3O(O2CCH2CH3)6(H2O)3]+, AS A NUTRITIONAL SUPPLEMENT OR IN TREATMENT OF MEDICAL CONDITIONS
UNIV ALABAMA20 citations90
US6197816B1Mar 6, 2001
Use of triaqua-mu3-oxohexakis-mu-propionatotrichromium (1+), [CR3O(O2CCH2CH3)6(H2O) 3]+, as a nutritional supplement or in treatment of medical conditions
UNIV ALABAMA19 citations90
US7354953B2Apr 8, 2008
Time-release compositions for delivery of [Cr3O(carboxylate)6(H2O)3]+
UNIV ALABAMA11 citations84
US6149948ANov 21, 2000
Method of decreasing plasma cholesterol and triglycerides with a chromium-containing complex
UNIV ALABAMA7 citations74
US6881752B2Apr 19, 2005
USE OF TRIAQUA-μ3-OXOHEXAKIS-μ-PROPIONATOTRICHROMIUM(1+), [CR3O(O2CCH2CH3)6(H2O)3]+, AS A NUTRITIONAL SUPPLEMENT OR IN TREATMENT OF MEDICAL CONDITIONS
UNIV ALABAMA10 citations71
US5872102AFeb 16, 1999
Method for isolation of bovine low-molecular weight CR-binding substance and method of use of the same
UNIV ALABAMA10 citations66
US7405313B2Jul 29, 2008
Method for the synthesis of basic chromium carboxylates
UNIV ALABAMA0 citations52
HOSPITAL FOR SICK CHILDREN
6 patentsUS12467093B2Nov 11, 2025
Biomarkers for autism spectrum disorders
HOSPITAL FOR SICK CHILDREN0 citations62
US11254984B2Feb 22, 2022
Biomarkers for autism spectrum disorders
HOSPITAL FOR SICK CHILDREN0 citations62
US10577658B2Mar 3, 2020
MECP2E1 gene
HOSPITAL FOR SICK CHILDREN0 citations51
US10577657B2Mar 3, 2020
MECP2E1 gene
HOSPITAL FOR SICK CHILDREN0 citations51
US10526653B2Jan 7, 2020
Biomarkers for autism spectrum disorders
HOSPITAL FOR SICK CHILDREN0 citations51
US9605314B2Mar 28, 2017
MECP2E1 gene
HOSPITAL FOR SICK CHILDREN0 citations51
VINCENT JOHN B
4 patentsUS8119351B2Feb 21, 2012
CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the same
VINCENT JOHN B4 citations71
US8598330B2Dec 3, 2013
CC2D2A gene mutations associated with joubert syndrome and diagnostic methods for identifying the same
VINCENT JOHN B2 citations60
US8716444B2May 6, 2014
Method and apparatus for predicting susceptibility to a developmental disorder
VINCENT JOHN B0 citations51
US8580502B2Nov 12, 2013
Methods of screening a subject for FHL1 mutations associated with novel X-linked muscular myopathies
VINCENT JOHN B0 citations44
CAMH
3 patentsUS7670773B2Mar 2, 2010
MECP2E1 gene
CAMH10 citations83
US9670544B2Jun 6, 2017
CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the same
CAMH0 citations51
US9096903B2Aug 4, 2015
CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the same
CAMH0 citations51